Alpha-1 Antitrypsin Deficiency – How It Works
Duration: 08:19
Alpha-1 Antitrypsin Deficiency (Alpha-1) is a genetic (inherited) condition – it is passed from parents to their children through their genes. Alpha-1 may result in serious lung disease in adults and/or liver disease at any age.
This video explains the causes, symptoms, diagnosis, treatment and pathology of Alpha-1 Antitrypsin Deficiency.
This video is brought to you by https://osmosis.org/. Along with providing open-access videos, Osmosis offers a comprehensive e-learning platform that connects med students.




